Combination therapy for treating disease
View Patent ↗Disclosed are methods for treating cancer comprising administering a xenotypic antibody and a chemotherapeutic drug to a patient suffering from cancer. Also disclosed is a method for inducing a host immune response in a patient against a multi-epitopic in vivo tumor antigen present in the host serum, which antigen does not elicit an effective host immune response, comprising administering to the patient a chemotherapeutic drug and a composition comprising a binding agent that specifically binds to a first epitope on the antigen and allowing the binding agent to form a binding agent/antigen pair, wherein an effective host immune response is elicited against a second epitope on the antigen.
1. A method for treating cancer, comprising administering to a patient suffering from cancer a chemotherapeutic drug, and a composition comprising an unlabeled xenotypic monoclonal antibody specific for a multi-epitopic in vivo antigen present in the patient's serum, wherein the multi-epitopic in vivo antigen is MUC-1, CA 1251, prostate specific antigen, CA 19.9, or TAG-72, wherein the chemotherapeutic drug is administered within a week of administering the composition.
2. The method of claim 1 , wherein the xenotypic monoclonal antibody is murine.
3. The method of claim 2 , wherein the xenotypic monoclonal antibody is selected from the group consisting of: Alt-1 which is producible by a hybridoma having ATCC deposit number PTA-975, Alt-2 which is producible by a hybridoma having ATCC deposit number PTA-1883, Alt-3 which is producible by a hybridoma having ATCC deposit number PTA-2691, Alt-4 which is producible by a hybridoma having ATCC deposit number PTA-2692, Alt-5 which is producible by a hybridoma having ATCC deposit number PTA-2690, and Alt-6 which is producible by a hybridoma having ATCC deposit number HB 12526.
4. The method of claim 1 , wherein the patient is a human.
5. The method of claim 1 or 3 , wherein the xenotypic monoclonal antibody in the composition is administered in a dose of less than or equal to 2 mg.
6. The method of claim 2 , further comprising surgically removing the cancer.
7. A method for treating cancer, comprising:
(1) surgically removing the cancer, and
(2) administering:
(a) a composition comprising an unlabeled xenotypic monoclonal antibody specific for a multi-epitopic in vivo antigen present in the patient's serum, said xenotypic monoclonal antibody is in a dose equal to or less than 2 mg, and,
(b) a chemotherapeutic drug,
wherein the chemotherapeutic drug is administered within a week of administering the composition.
8. The method of claim 7 , wherein the xenotypic monoclonal antibody is selected from the group consisting of: Alt-1 which is producible by a hybridoma having ATCC deposit number PTA-975, Alt-2 which is producible by a hybridoma having ATCC deposit number PTA-1883, Alt-3 which is producible by a hybridoma having ATCC deposit number PTA-2691, Alt-4 which is producible by a hybridoma having ATCC deposit number PTA-2692, Alt-5 which is producible by a hybridoma having ATCC deposit number PTA-2690, and Alt-6 which is producible by a hybridoma having ATCC deposit number HB 12526.
9. The method of claim 7 , wherein administration of the composition comprises a 20 minute intravenous infusion.
10. A method for treating cancer in a patient, comprising:
(1) surgically removing the cancer, and
(2) administering a composition comprising an unlabeled xenotypic monoclonal antibody at weeks 1, 3, 5, 7 and 9, followed by concurrently administering a chemotherapeutic drug and the composition, said xenotypic monoclonal antibody in the composition is administered in a dose less than or equal to 2 mg at week 12.
11. The method of claim 9 , wherein the xenotypic monoclonal antibody is selected from the group consisting of: Alt-1 which is producible by a hybridoma having ATCC deposit number PTA-975, Alt-2 which is producible by a hybridoma having ATCC deposit number PTA-1883, Alt-3 which is producible by a hybridoma having ATCC deposit number PTA-2691, Alt-4 which is producible by a hybridoma having ATCC deposit number PTA-2692, Alt-5 which is producible by a hybridoma having ATCC deposit number PTA-2690, and Alt-6 which is producible by a hybridoma having ATCC deposit number HB 12526.
12. A method for inducing a host immune response in a patient against a multi-epitopic in vivo tumor antigen comprising administering to the patient a chemotherapeutic drug and a composition comprising an unlabeled monoclonal antibody or a fragment thereof that specifically binds to a first epitope on the antigen and allowing the monoclonal antibody or fragment thereof to form a monoclonal antibody or fragment thereof / antigen pair, wherein a host immune response is elicited against a second epitope on the antigen, wherein antigen is selected from the group consisting of MUC-1, CA 125, prostate specific antigen, CA 19.9 or TAG-72, wherein said antigen does not elicit an effective host immune response, wherein the chemotherapeutic drug is administered within a week of administering the monoclonal antibody and wherein the monoclonal antibody is selected from the group consisting of: Alt-1 which is producible by a hybridoma having ATCC deposit number PTA-975, Alt-2 which is producible by a hybridoma having ATCC deposit number PTA-1883, Alt-3 which is producible by a hybridoma having ATCC deposit number PTA-2691, Alt-4 which is producible by a hybridoma having ATCC deposit number PTA-2692, Alt-5 which is producible by a hybridoma having ATCC deposit number PTA-2690, and Alt-6 which is producible by a hybridoma having ATCC deposit number RB 12526.
13. The method of claim 12 , wherein the monoclonal antibody is a murine xenotypic monoclonal antibody.
14. The method of claim 12 , wherein the patient is human.
15. The method of claim 12 , wherein the antibody is administered in a dose of equal to or less than 2 mg.
16. The method of claim 12 , further comprising surgically removing the cancer.
17. A method for treating cancer, comprising administering a chemotherapeutic drug, an antigen, and a monoclonal antibody or a fragment thereof that binds the antigen, wherein the chemotherapeutic drug is administered within a week of administering the monoclonal antibody and wherein the monoclonal antibody is selected from the group consisting of: Alt-1 which is producible by a hybridoma having ATCC deposit number PTA-975, Alt-2 which is producible by a hybridoma having ATCC deposit number PTA-1883, Alt-3 which is producible by a hybridoma having ATCC deposit number PTA-2691, Alt-4 which is producible by a hybridoma having ATCC deposit number PTA-2692, Alt-5 which is producible by a hybridoma having ATCC deposit number PTA-2690, and Alt-6 which is producible by a hybridoma having ATCC deposit number HB 12526.
18. The method of claim 17 , wherein the patient is human.
19. The method of claim 17 , wherein the antibody is administered in a dose of equal to or less than 2 mg.
20. The method of claim 17 , wherein the monoclonal antibody is a murine monoclonal antibody.